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奥马珠单抗治疗儿童变应性(IgE 介导)哮喘的安全性和耐受性。

Safety and tolerability of omalizumab in children with allergic (IgE-mediated) asthma.

机构信息

Department of Pediatrics, University of Colorado Health Sciences Center, National Jewish Health, Denver, CO 80206, USA.

出版信息

Curr Med Res Opin. 2011 Jan;27(1):163-9. doi: 10.1185/03007995.2010.539502. Epub 2010 Dec 2.

Abstract

OBJECTIVE

This pooled analysis assessed the safety of omalizumab in children with allergic (immunoglobulin E-mediated) asthma.

STUDY DESIGN

Two double-blind, placebo-controlled studies in children (6 to < 12 years) with moderate-to-severe allergic asthma investigated the efficacy/safety of omalizumab. Children on optimized asthma care (inhaled corticosteroids ± other controller medications) were randomized (2:1) to omalizumab (75-375  mg  sc, q2 or q4 wk) or placebo. Pooled safety findings from these trials are presented in this publication.

RESULTS

The safety population included 926 children (omalizumab, n = 624; placebo, n = 302). Adverse events (AEs) were more frequently reported in the placebo (91.7%) than omalizumab (89.7%) group. The most common AEs were nasopharyngitis, upper respiratory tract infection and headache. Suspected treatment-related AEs included headache, erythema and urticaria; none of which were reported by ≥ 2% of patients receiving omalizumab. Serious AEs (SAEs) were reported by 3.4% and 6.6% of patients receiving omalizumab and placebo, respectively; the most common were appendicitis, pneumonia and bronchitis; no deaths were reported.

CONCLUSIONS

Omalizumab has an acceptable safety profile, with a risk of AEs similar to placebo. This, combined with its efficacy profile, suggests that omalizumab may provide an additional asthma management option for children (6 to < 12 years) uncontrolled with current therapy that follows established guidelines.

摘要

目的

本汇总分析评估奥马珠单抗在过敏性(免疫球蛋白 E 介导)哮喘儿童中的安全性。

研究设计

两项针对中重度过敏性哮喘儿童的双盲、安慰剂对照研究评估了奥马珠单抗的疗效/安全性。接受优化哮喘护理(吸入皮质类固醇+其他控制药物)的儿童按 2:1 随机分配至奥马珠单抗(75-375mg sc,每 2 或 4 周 1 次)或安慰剂组。本出版物介绍了这些试验的汇总安全性发现。

结果

安全性人群包括 926 名儿童(奥马珠单抗组 n=624,安慰剂组 n=302)。安慰剂组(91.7%)比奥马珠单抗组(89.7%)更频繁报告不良事件(AE)。最常见的 AE 是鼻咽炎、上呼吸道感染和头痛。疑似与治疗相关的 AE 包括头痛、红斑和荨麻疹;接受奥马珠单抗治疗的患者中没有任何一种 AE 的报告比例≥2%。奥马珠单抗组和安慰剂组分别有 3.4%和 6.6%的患者报告了严重不良事件(SAE);最常见的是阑尾炎、肺炎和支气管炎;没有报告死亡。

结论

奥马珠单抗具有可接受的安全性,其 AE 风险与安慰剂相似。这与它的疗效特征相结合,表明奥马珠单抗可能为不符合既定指南的当前治疗方案控制不佳的儿童(6 至<12 岁)提供一种额外的哮喘管理选择。

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